Taiwan FDA registration 49e7aa152f619268d98f82e281c1b2c5
"Siemens" chemical corrective
TW: “西門子”化學校正品
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered Mar 02, 2009 – Mar 02, 2029ActiveRegistration details
- Analysis ID
- 49e7aa152f619268d98f82e281c1b2c5
- Customs Code
- DHA00601995701
Company information
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- In vitro diagnostic tests for correcting biochemical analysis systems including ADVIA biochemical analysis systems to detect biochemical analysis tests.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Mar 02, 2009
- Expiry Date
- Mar 02, 2029
About this record
Access comprehensive regulatory information for "Siemens" chemical corrective in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49e7aa152f619268d98f82e281c1b2c5 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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